Stellenangebote für Requirements Manager Jobs in Basel Stadt Kanton

15.06.25 | Vollzeit | Basel-Stadt | JobLeads GmbH | CHF 125’000 - CHF 150’000 With Patient Safety, ensures continuous evaluation of drug safety profile, including safety monitoring of clinical studies and signal detection from post-marketing surveillance. Serves as a core member of the Safety Management Team (SMT) - As the medical expert, leads interactions with external stakeholders

15.06.25 | Vollzeit | Basel (Basel-Stadt) | JobLeads GmbH | CHF 80’000 - CHF 100’000 Pro-actively monitor, manage and improve quality through specific metrics, customer satisfaction and issue resolution - Identify risk areas & build and manage contingency to mitigat - Identify new market opportunities - Manage sales pipeline and track KPIs Relationship management . Requirements

15.06.25 | Vollzeit | Basel (Basel-Stadt) | JobLeads GmbH | CHF 100’000 - CHF 125’000 Growth at optimal margins. Hence the central AA team is an integral part of the Strategy Management Office at EPD that has a very close link and regular interactions with the EPD Senior Leadership Team. With the above requirements in mind, EPD is looking to fill a role of a Manager AA Cloud, reporting

14.06.25 | Vollzeit | Basel (Basel-Stadt) | JobLeads GmbH | CHF 80’000 - CHF 100’000 Of injectable medicines. - Strong knowledge of GMP regulations and quality standards. - Experience with managing discrepancies, changes, and using management systems like SAP and LIMS. - Proficient in English and German communication. - Ability to learn quickly, work well in teams, and manage multiple tasks

14.06.25 | Vollzeit | Basel (Basel-Stadt) | JobLeads GmbH | CHF 80’000 - CHF 100’000 Experience in a Pharmaceutical Technical Development environment. - Knowledge of cGMP and Quality requirements for clinical development stages of biotechnological and/or parenteral IMPs (e.g. EU Annex 1). - Experience in Discrepancy Management, CAPA, Technical Change Management (Veeva Vault

14.06.25 | Vollzeit | Basel (Basel-Stadt) | JobLeads GmbH | CHF 80’000 - CHF 100’000 Assessments and risk management documentation. - Forecast and plan resource demands for device development projects. Execute projects within the agreed time, quality and cost constraints, resulting in state-of-the-art drug delivery devices - Apply knowledge of the regulatory landscape to ensure standard

28.05.25 | Vollzeit | Basel (Basel-Stadt) | Oxford Global ResourcesContribute to lab organization by managing inventory, consumables, and maintaining a clean workspace - Support drafting and updating of equipment and instrument SOPs - Participate in process improvements and lab optimization projects - Assist with on-site audits and ensure the lab meets inspection readiness

12.06.25 | Vollzeit | Basel (Basel-Stadt) | JobLeads GmbH | CHF 200’000 - CHF 250’000 And develop clinical documents like, clinical study protocols and amendments and review other clinical documents like safety management plan, medical monitoring plan - Work closely with colleagues from Clinical Operations and Clinical Biomarker department to deliver clinical study program goals and milestones

12.06.25 | Vollzeit | Basel (Basel-Stadt) | JobLeads GmbH | CHF 80’000 - CHF 100’000 To a variety of audiences. - Knowledge of current requirements and guidelines applicable to submission documents. - Excellent writing skills. - Excellent interpersonal and oral communication skills. - Strong knowledge of MS Word and Outlook, some knowledge of Excel and PowerPoint. - Project management

12.06.25 | Vollzeit | Basel (Basel-Stadt) | JobLeads GmbH | CHF 80’000 - CHF 100’000 Knowledge of cGMP and Quality requirements for clinical development stages of biotechnological and - or parenteral IMPs (e.g. EU Annex 1). - Experience in Discrepancy Management, CAPA, Technical Change Management (Veeva Vault) and Manufacturing Management (SAP), MES (PMX) and LIMS is an additional plus